Senior or Principal Regulatory Medical Writer

Would you like to join one of the fastest-growing organizations with a stated goal of using latest and
greatest AI, GenAI, LLM, Cloud and Digital Technologies to advance drug development and improve
patient care pathways. Write Med.

AI helps Biopharma and Life Sciences Companies, among others, to
reduce the time for writing medical publications and regulatory documents. Our Medical Writing Team
support our customers’ missions with creative and transformative spirit of innovation across all
therapeutic areas.

This is an opportunity to be a Principal or Senior Medical Writer, to guide our AI Architects, Data
Scientists and Engineers towards medical writer needs, evaluate and improve the quality of outputs, and
be the voice of the customers internally.

• This position will be a remote position, with occasional ( approximately 10-20%) travel to client
  sites and conferences
• Doctoral Degree (MD, PhD, Pharm
  
  D or equivalent) in life sciences or related discipline, and 10+
  years of work experience in academia or industry with at least 5+ years of medical writing work
  experience in the industry
• Or, M.S. Degree and 15+ years of experience with at least 7+ years of medical writing work
  experience in the industry
• Extensive experience writing 4 or more of the following: IND components, Clinical Study
  Reports, Protocols, Investigator Brochures, Informed Consent Forms, 510
  
  Ks, NDAs
• Strong ability to accurately interpret or check interpretation of statistical findings
• 5+ years of experience fact-checking references, statistical interpretation, and consistency
• Experience writing in accordance with AMA manual of style
• 10+ years of experience using Pub Med and Endnote (or Endnote equivalent)
• Complete/Native fluency in English language
• Thorough understanding of US Healthcare landscape

• Professional oral and written communication skills, presenting to an audience containing one or
  more executive team members
• Familiarity with Information Technology or AI applications in regulatory medical writing
• Experience applying technical or scientific expertise to identify, balance trade-offs, and solve
  difficult challenges

• Fact-check AI generated documents for accuracy with respect to reference and data
  interpretation and summary, as well as adherence to AMA manual of style. Provide statistical
  summary of document quality
• Assist in training our AI Systems and enriching our database
• Be the voice of the customers for AI Product Development teams
• Interface with Information Technology / AI team to align product development with latest needs
  of medical writers across the globe
• Suggest improvements to AI generated medical documents, so as to achieve outstanding
  document quality, accuracy, and style
• Be the regulatory writing SME
• Our benefits help you thrive personally and professionally, from wellness programs and tuition
  reimbursement to expense reimbursement programs that can be used for needs that best suit
  you and your family, from student loan repayment, to childcare, to pet insurance
• Our inclusive culture, active and engaged employee resource groups, and caring leaders value
  every voice and support you in doing the best work of your career
• The pay range for this position is $160,000 to $190,000, however, base pay offered may vary
  depending on skills, experience, job-related knowledge and location
• This position is also eligible for a short-term incentive and a long-term incentive as part of total
  compensation